Synthesis and Properties of Rhodium(III) Porphyrin Cyclic Tetramer and Cofacial Dimer

Rhodium(lll) porphyrin complexes, [Rh(4-PyT3P)CI]4 (1) and [Rh(2-PytB3P)CI]2 (2) (4-PyT3P = 5-(4-pyridyl)-10,15,20-tritolylporphyrinato dianion, 2-PytB3P = 5-(2-pyridyl)-10,15,20-tri(4-terf-butyl)phenylporphyrinato dianion), were self-assembled and characterized by H nuclear magnetic resonance spectroscopy, infrared spectroscopy, and electron spray ionization-mass spectroscopy methods. The spectroscopic results certified that the rhodium porphyrin complexes 1 and 2 have a cyclic tetrameric structure and a cofacial dimeric structure, respectively. The X-ray structure analysis of 1 confirmed the cyclic structure of the complex. The Soret bands of both oligomers were significantly broadened by excitonic interactions between the porphyrin units, compared to those observed for a corresponding analogue of Rh(TTP)(Py)CI (TTP = 5,10,15,20-tetratolylporphyrinato dianion, Py == pyridine). Stepwise oxidation of the porphyrin rings in the oligomers was observed by cyclic voltammetry. The oligomers 1 and 2 are very stable in solution, and they slowly undergo reactions with pyridine to give corresponding monomer complexes only at high temperatures (~80 °C).